Members Free CME - Autosomal Recessive Axonal Neuropathy with Neuromyotonia is an advanced level case study, appropriate for fellows and practicing physicians. Presenting symptoms in this case study include distal leg and arm weakness and difficulty releasing grasp. Upon completion of this case study, participants will acquire skills to:
1) Apply clinical and electrodiagnostic (EDX) criteria to narrow the differential diagnosis
2) Recognize the clinical and EDX features of an axonal motor neuropathy
3) Identify the clinical and EDX characteristics related to myokymic and neuromyotonic discharges
4) Recognize a recently-described new form of Charcot–Marie–Tooth disease


ACCREDITATION STATEMENT
The AANEM is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians.

CREDIT DESIGNATION
The AANEM designates this enduring material for a maximum of 2 AMA PRA Category 1 Credits ^TM. Physicians should claim only the credit commensurate with the extent of their participation in the activity. Credit expires 9/12/2019.

DISCLOSURE INFORMATION 
All authors and planners of this activity had nothing to disclose.

FORMAT: PDF

Ludwig Gutmann, MD, Tiffany Grider, MS, CGC, Nivedita Jerath, MD, and Michael Shy, MD